Evidence map›Paper›PMID 29340013›Full record

ArticleOncotarget2017

The small molecule SI113 synergizes with mitotic spindle poisons in arresting the growth of human glioblastoma multiforme.

Claudia Abbruzzese, Giada Catalogna, Enzo Gallo, Simona di Martino, Anna M Mileo, Mariantonia Carosi, Vincenzo Dattilo, Silvia Schenone, Francesca Musumeci, Patrizia Lavia and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Drug repurposing against COVID-19: focus on anticancer agents.Journal of experimental & clinical cancer research : CR · 2020
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  19. Reprogramming glioblastoma multiforme cells into neurons by protein kinase inhibitors.Journal of experimental & clinical cancer research : CR · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Claudia AbbruzzeseDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Cellular Networks and Therapeutic Targets, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Giada CatalognaDepartment of "Scienze della Salute", University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Enzo GalloDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Pathology, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Simona di MartinoDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Pathology, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Anna M MileoDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Tumor Immunology and Immunotherapy, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Mariantonia CarosiDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Pathology, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Vincenzo DattiloDepartment of "Scienze della Salute", University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Silvia SchenoneDepartment of Pharmacy, University of Genova, Genova, Italy.
Francesca MusumeciDepartment of Pharmacy, University of Genova, Genova, Italy.
Patrizia LaviaInstitute of Molecular Biology and Pathology (IBPM), National Research Council of Italy (CNR), c/o University "La Sapienza", Rome, Italy.
Nicola PerrottiDepartment of "Scienze della Salute", University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Rosario AmatoDepartment of "Scienze della Salute", University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Marco G PaggiDepartment of Research, Advanced Diagnostics and Technological Innovation, Unit of Cellular Networks and Therapeutic Targets, "Regina Elena" National Cancer Institute, IRCCS, Rome, Italy.
Magna Graecia University · ITNational Cancer Institute · MYExpert System (Italy) · ITUniversity of Genoa · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the deadliest brain tumor. State-of-art GBM therapy often fails to ensure control of a disease characterized by high frequency of recurrences and progression. In search for novel therapeutic approaches, we assayed the effect of compounds from a cancer drug library on the ADF GBM cell line, establishing their elevated sensitivity to mitotic spindle poisons. Our previous work showed that the effectiveness of the spindle poison paclitaxel in inhibiting cancer cell growth was dependent on the expression of RANBP1, a regulatory target of the serine/threonine kinase SGK1. Recently, we developed the small molecule SI113 to inhibit SGK1 activity. Therefore, we explored the outcome of the association between SI113 and selected spindle poisons, finding that these drugs generated a synergistic cytotoxic effect in GBM cells, drastically reducing their viability and clonogenic capabilities

Indexed as

glioblastoma multiformein vivo cancer therapySGK1SI113vincristine

Identifiers

PMID29340013
PMCPMC5762281
OpenAlexW2770643480

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.